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10 Possible Causes for Acidosis, Kussmaul Respiration, Persistent Lactic Acidosis

  • Lactic Acidosis

    […] and metabolic acidosis.[symptoma.com] […] interval: 2.5-20.6; P CONCLUSION: In the absence of risk factors associated with persistent lactic acidosis, such as shock or acute kidney or liver injury, continued peri-operative[ncbi.nlm.nih.gov] lactic acidosis CAUSES (Cohen & Woods classification) Type A – Inadequate Oxygen Delivery anaerobic muscular activity (sprinting, generalised convulsions) tissue hypoperfusion[lifeinthefastlane.com]

  • Acidosis

    Nervous system involvement may be seen with acidosis and occurs more often with respiratory acidosis than with metabolic acidosis.[en.wikipedia.org] Hyperlactatemia is defined as a persistent, mild to moderate (2-4 mmol/L) increase in blood lactate concentration without metabolic acidosis , whereas lactic acidosis is characterized[emedicine.medscape.com] ., dyspnea, marked Kussmaul respirations) These patients generally have severe metabolic acidosis with respiratory compensation.[emcrit.org]

  • Alpers Syndrome

    Skeletal muscle did not contain ragged red fibers, nor were there mitochondrial DNA point mutations characteristic for mitochondrial encephalomyopathy, lactic acidosis, and[ncbi.nlm.nih.gov] acidosis, and strokelike episodes syndrome (MELAS) during recurrent status epilepticus ( 14 ).[ajnr.org] クスマウル Kussmaul respiration クスマウル大呼吸 AdolfKussmaul (1822-1902) Germaninternist Kveim クベイム反応 Kveim reaction クベイム反応 MortenAnsgar Kveim (1892-1966) Norwegian pathologist Ladd[jams.med.or.jp]

  • Sepsis

    The patient had severe metabolic acidosis with elevated lactate upon arrival to the emergency department.[ncbi.nlm.nih.gov] Hypotension and/or Kussmaul’s respirations in severe acidosis that are present in the septic patient may lead to peri-intubation arrest if not recognized and managed prior[clinicaladvisor.com] Hypoperfusion abnormalities may include lactic acidosis, oliguria, or an acute alteration in mental status.[doi.org]

  • Congenital Lactic Acidosis

    We report an inborn error of the tricarboxylic acid cycle, alpha-ketoglutarate dehydrogenase deficiency, in three siblings with hypotonia, metabolic acidosis, and hyperlactatemia[ncbi.nlm.nih.gov] Case 2 (personal communication) 20 An 11 year old girl with MELAS had persistent lactic acidosis (venous blood lactate 5 mmol/l), growth retardation, muscular fatigue, and[adc.bmj.com] respiration E87.2 Lacticemia, excessive E87.2 Retention - see also Retained carbon dioxide E87.2 ICD-10-CM Codes Adjacent To E87.2 E85.82 Wild-type transthyretin-related[icd10data.com]

  • Mauriac's Syndrome

    Acidosis Pediatric Metabolic Alkalosis Pediatric Pellagra Pediatric Respiratory Acidosis Pediatric Respiratory Alkalosis Pediatric Short Bowel Syndrome Rickets Imaging Silver-Russell[emedicine.staging.medscape.com] A Rare Case of Persistent Lactic Acidosis in the ICU: Glycogenic Hepatopathy and Mauriac Syndrome. Case Rep Crit Care. 2016; 2016: 6072909.[journals.viamedica.pl] ’s respiration) Acetone, formed by nonenzymatic conversation of acetoacetate, is responsible for the characteristic fruity odor of the breath 58 Ketones are readily excreted[slideplayer.com]

  • Severe Infantile Carnitine Palmitoyl Transferase II Deficiency

    Infants will try to correct metabolic acidosis by a reflex respiratory alkalosis using hyperventilation and Kussmaul respirations.[mhmedical.com] lactic acidosis Mitochondrial encephalopathy Attention deficit hyperactivity disorder Pallor Abnormality of the abdominal wall Psychosis Involuntary movements Drooling Abnormality[mendelian.co] The enzyme deficiencies that give rise to congenital lactic acidosis can potentially affect many different organ systems of the body and, therefore, lead to a wide variety[mitoaction.org]

  • Lethal Neonatal Carnitine Palmitoyl Transferase II Deficiency

    Infants will try to correct metabolic acidosis by a reflex respiratory alkalosis using hyperventilation and Kussmaul respirations.[mhmedical.com] The enzyme deficiencies that give rise to congenital lactic acidosis can potentially affect many different organ systems of the body and, therefore, lead to a wide variety[mitoaction.org] Initial laboratory evaluation revealed significant metabolic acidosis, elevated plasma lactic acid (5 mmol/L; normal, 0.6–2.5), elevated serum CK (700 U/L; normal, 30–220)[the-rheumatologist.org]

  • Behr Syndrome

    The clinical features include nonspecific speech and language delay without metabolic derangement in some individuals and with hypoglycemia and metabolic acidosis in others[ncbi.nlm.nih.gov] クスマウル Kussmaul respiration クスマウル大呼吸 AdolfKussmaul (1822-1902) Germaninternist Kveim クベイム反応 Kveim reaction クベイム反応 MortenAnsgar Kveim (1892-1966) Norwegian pathologist Ladd[jams.med.or.jp] The concomitant acidosis may also have played an important part because of its similar effect in decreasing INa currents 66,67 .[elsevier.pt]

  • Waardenburg Syndrome Type 2E

    […] with deafness ( ATP6B1) Renal tubular acidosis, distal, AD ( SLC4A1) Renal tubular acidosis, distal, AR ( SLC4A1) Renal tubular acidosis, distal, autosomal recessive ( ATP6V0A4[en.praenatal-medizin.de] クスマウル Kussmaul respiration クスマウル大呼吸 AdolfKussmaul (1822-1902) Germaninternist Kveim クベイム反応 Kveim reaction クベイム反応 MortenAnsgar Kveim (1892-1966) Norwegian pathologist Ladd[jams.med.or.jp] Kearns-Sayre syndrom, progressive external ophthalmoplegia, Pearson syndrome, myoclonic epilepsy with ragged red fibers (MERFF), mitochondrial encephalomyopathy with lactic acidosis[orphananesthesia.eu]

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